ichthyosis的例句大全

Q& A on Sex Epidermolytic hyperkeratosis ichthyosis complicated by dwarf: a case report

表皮松解性角化过度鱼鳞病伴侏儒1例

Prenatal exclusion of harlequin ichthyosis; potential pitfalls in the timing of the fetal skin biopsy

产前排除丑角样鱼鳞病：择时胎儿皮肤活检的潜在缺陷

Double blind randomized controlled clinical trial of lactic acid compound ointment in the treatment of ichthyosis vulgaris

复方乳酸软膏治疗寻常型鱼鳞病随机双盲基质对照多中心临床研究

Fishskin disease Expressions of genes associated with growth and differentiation in peripheral blood leukocytes of lamellar ichthyosis patients

板层状鱼鳞病患者外周血白细胞生长、分化相关基因的表达

Objective To elucidate the pathogenic genes in a pedigree with autosomal dominant ichthyosis vulgaris ( IV).

目的研究一常染色体显性遗传寻常型鱼鳞病家系的致病基因。

The diagnosis was ichthyosis in histopathological examination, congenital nerve deaf-mutism in otolaryngology and corneal pannus in ophthalmology.

躯干部皮肤明显干燥，皮肤角化过度，呈皮革样变化。病理活检为鱼鳞病，耳科检查为先天感音神经性耳聋，眼科检查为角膜血管翳。

these vary in size, some being fine, delicate, and branny, as in eczema and ichthyosis, while still others are stratified, as in psoriasis.

鳞屑大小不一，有的细小如糠状，如湿疹和鱼鳞病的鳞屑；还有的成层状，如银屑病的鳞屑。

this disease is characterized by limb length discrepancies, growth retardation, ichthyosis, cataracts, and punctate calcification.

这种疾病的特点是下肢长度差异，生长迟缓，鱼鳞病，白内障，和点状钙化。

ultrastructural alterations of the stratum corneum lipids in patients with lamellar ichthyosis

板层状鱼鳞癣病人角质层脂质超微结构的观察

Harlequin ichthyosis ( HI ) is a severe subtype of autosomal recessive congenital ichthyoses ( ARCI ) .

丑角样鱼鳞病是常染色体隐性遗传性鱼鳞病的一种严重 亚型.

Keratitis, ichthyosis , and deafness syndrome ( KID syndrome ) is a rare congenital disorder disease.

目的观察角膜炎 、 鱼鳞病、耳聋 综合征 的临床表现.

Excessive or abnormal dryness of the skin, as in ichthyosis.

干皮''.'病'.''皮肤异常或不正常的''.'干燥'. '', 如鱼鳞癣.

Objective To elucidate the pathogenic genes in a pedigree with autosomal dominant ichthyosis vulgaris ( IV ) .

目的研究一常染色体显性遗传寻常型鱼鳞 病家 系的致病基因.

Objective To detect the activity of transglutaminase 1 ( TGM 1 ) and gene mutation in a family with lamellar ichthyosis.

目的检测一板层状鱼鳞病家系中患者转谷氨酰胺酶1的活性及其编码基因的突变.

On admission he was found to have widespread congenital ichthyosis.

入院时发现,其身体多处患有先天性鳞癣,热度已消,但颈部、下和腹股沟淋巴腺仍肿大,脾缘可触及.